| Literature DB >> 33395306 |
Bingling Lin1,2, Liejing Lu1, Yong Wang3, Qinyuan Zhang1, Zhe Wang1, Guanxun Cheng2, Xiaohui Duan1, Fang Zhang1, Mingwei Xie1, Hongbo Le1, Xintao Shuai4, Jun Shen1.
Abstract
Transplantation of neural stem cells (NSCs) is a promising treatment paradigm to replace lost neurons and reconstruct the damaged neural circuit after ischemic stroke. However, most transplanted NSCs often differentiate into astrocytes rather than functional neurons, and the poor neuronal differentiation adversely affects the therapeutic outcome of NSCs and limits their clinical translation for stroke therapy. Herein, a theranostic nanomedicine is developed to codeliver superparamagnetic iron oxide nanoparticles (SPIO) and small interfering RNA/antisense oligonucleotides (siRNA/ASO) against Pnky long noncoding RNA (lncRNA) into NSCs. This nanomedicine not only directs neuronal differentiation of NSCs through silencing the Pnky lncRNA but also allows an in vivo tracking of NSCs with magnetic resonance imaging. The enhanced neuronal differentiation of NSCs significantly improved the structural and functional recovery of the damaged brain after a stroke. The results demonstrate the great potential of the multifunctional nanomedicine targeting lncRNA to enhance stem cell-based therapies for a stroke.Entities:
Keywords: ischemic stroke; long noncoding RNA; magnetic resonance imaging; multifunctional nanomedicine; neural stem cell transplantation
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Year: 2021 PMID: 33395306 DOI: 10.1021/acs.nanolett.0c04560
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189